A novel p.R890C mutation in EPHA2 gene associated with progressive childhood posterior cataract in a Chinese family

A novel p.R890C mutation in EPHA2 gene associated with progressive childhood posterior cataract in a Chinese family

<b>AIM:</b>To identify the genetic defect in a Chinese family with bilateral progressive childhood posterior cataract.<b>METHODS:</b> A two-generation family was recruited in this study. Family history and clinical data were recorded. All reported candidate genes associated w...

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Bibliographic Details
Main Author: Xing-Chao Shentu
Format: Article
Language:English
Published: Press of International Journal of Ophthalmology (IJO PRESS) 2013-02-01
Series:International Journal of Ophthalmology
Subjects:
EPHA2
gene mutation
posterior cataract
Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3580246/

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